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Water → ethyl 2-[2-(Boc-L-alanyl)aminothiazol-4-yl]glyoxylate

HRID 274241
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 274241
[NH2:1][C:2]1[S:3][CH:4]=[C:5]([C:7](=[O:13])[C:8]([O:10][CH2:11][CH3:12])=[O:9])[N:6]=1.[C:14]([NH:21][C@H:22]([C:24](O)=[O:25])[CH3:23])([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15].Cl.C(N=C=NCCCN(C)C)C.O>CN(C)C=O.CN(C)C1C=CN=CC=1>[C:14]([NH:21][C@H:22]([C:24]([NH:1][C:2]1[S:3][CH:4]=[C:5]([C:7](=[O:13])[C:8]([O:10][CH2:11][CH3:12])=[O:9])[N:6]=1)=[O:25])[CH3:23])([O:16][C:17]([CH3:18])([CH3:20])[CH3:19])=[O:15]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 962WaterHCID 85082Tert-butoxycarbonylalanineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 4356513Ethyl 2-(2-Amino-4-thiazolyl)-2-oxoacetate

Produkt 1

HCID 18659161ethyl 2-[2-(Boc-L-alanyl)aminothiazol-4-yl]glyoxylateAusbeute 71,4 %

Reagenzien, Katalysatoren, Lösungsmittel

2
HCID 142844-(Dimethylamino)pyridineKatalysatorHCID 6228DimethylformamideLösungsmittel2×

Versuchsvorschrift

Ethyl 2-(2-aminothiazol-4-yl)glyoxylate (4.0 g) and Boc-L-alanine (5.67 g) were dissolved in 40 ml of N,N-dimethylformamide (hereafter abbreviated as DMF), and thereto was added 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide hydrochloride (5.74 g) under ice-cooling followed by addition of 4-dimethylaminopyridine (0.4 g). The mixture was stirred at room temperature for 5 hours. Water (400 ml) was added thereto, and the mixture was extracted twice with ethyl acetate (300 ml). The ethyl acetate layer was washed with 10% aqueous solution of citric acid (200 ml), saturated aqueous solution of sodium bicarbonate (200 ml) and saturated brine (200 ml) in this order, and dried over anhydrous sodium sulfate. The ethyl acetate was distilled off under reduced pressure, and the residue was subjected to silica gel column chromatography eluted with benzene-ethyl acetate. The object fraction was concentrated to give 5.30 g of ethyl 2-[2-(Boc-L-alanyl)aminothiazol-4-yl]glyoxylate.

Aufarbeitung

  1. temperaturecooling
  2. extractionthe mixture was extracted twice with ethyl acetate (300 ml)
  3. washThe ethyl acetate layer was washed with 10% aqueous solution of citric acid (200 ml), saturated aqueous solution of sodium bicarbonate (200 ml) and saturated brine (200 ml) in this order
  4. dry with materialdried over anhydrous sodium sulfate
  5. distillationThe ethyl acetate was distilled off under reduced pressure
  6. washeluted with benzene-ethyl acetate
  7. concentrationThe object fraction was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-f36417eb0f2945ac991ee10e1df38efd
Quelldatensatz
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05389625

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